- Cat. No.
- A10495
Kaempferol
Kaempferol is found to inhibit bovine aorta myosin light chain kinase with a Ki of 0.3-0.5 microM and also is found to inhibit VEGF expression and in vitro angiogenesis through a novel ERK-NFκB-cMyc-p21 pathway.
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Myosin inhibitors and activators act on the actin-based motor proteins of muscle and non-muscle cells. Myosins hydrolyze adenosine triphosphate (ATP) and convert that chemical energy into movement along actin filaments. Blebbistatin was introduced in 2003 as a selective inhibitor of non-muscle myosin II and is used to study cytokinesis and cortical tension. The catalogue lists it as (-)-Blebbistcitin together with para-Nitroblebbistatin, a photostable analog suited to imaging experiments. Omecamtiv mecarbil works in the opposite direction and accelerates the cardiac myosin ATPase cycle. ML 7 hydrochloride and ML-9 hydrochloride act upstream on myosin light chain kinase, as does the neighboring MLCK category.
Kaempferol is found to inhibit bovine aorta myosin light chain kinase with a Ki of 0.3-0.5 microM and also is found to inhibit VEGF expression and in vitro angiogenesis through a novel ERK-NFκB-cMyc-p21 pathway.
Synonyms: MYK461; SAR439152
Mavacamten is a modulator of cardiac myosin, with IC50s of 490, 711 nM for bovine cardiac and human cardiac, respectively.
Myosin Modulator 1 is a selective modulator of myosin that inhibits ATPase activity in rabbit psoas, porcine atrial, and porcine ventricular tissues, exhibiting IC25 values of 0.42, 0.13, and 3.09 μM, respectively. This compound plays a significant role in regulating systolic cardiac performance, making it a valuable tool for research in cardiac physiology and myosin-related studies.
Myosin Modulator 2 (Compound B172) is a modulator of myosin that selectively inhibits ATPase activity in rabbit psoas muscle, porcine atria, and porcine ventricles, with IC25 values of 2.013 μM, 2.94 μM, and 20.93 μM, respectively. This compound demonstrates significant regulation of systolic cardiac performance in Sprague Dawley rats, making it a valuable tool in cardiac physiology research and drug development studies focusing on muscle contractility and cardiovascular function.